Welcome, Guest. Please login or register.
December 27, 2024, 09:17:29 am

Login with username, password and session length


Members
  • Total Members: 6315
  • Latest: DRG
Stats
  • Total Posts: 55137
  • Total Topics: 4855
  • Online Today: 251
  • Online Ever: 3061
  • (September 25, 2024, 11:40:40 pm)
Users Online
Users: 0
Guests: 218
Total: 218

Welcome

Welcome to the Hep Forums, a round-the-clock discussion area for people who have Fatty Liver Disease, Hepatitis B, C or a co-infection, their friends and family and others with questions about hepatitis and liver health. Check in frequently to read what others have to say, post your comments, and hopefully learn more about how you can reach your own health goals.

Privacy Warning: Please realize that these forums are open to all, and are fully searchable via Google and other search engines. If this concerns you, then do not use a username or avatar that are self-identifying in any way. We do not allow the deletion of anything you post in these forums, so think before you post.
  • The information shared in these forums, by moderators and members, is designed to complement, not replace, the relationship between an individual and his/her own physician.
  • All members of these forums are, by default, not considered to be licensed medical providers. If otherwise, users must clearly define themselves as such.
  • Product advertisement (including links); banners; and clinical trial, study or survey participation—is strictly prohibited by forums members unless permission has been secured from the Hep Forum Moderators.
Finished Reading This? You can collapse this or any other box on this page by clicking the symbol in each box.

Author Topic: hello new to the board  (Read 8425 times)

0 Members and 2 Guests are viewing this topic.

Offline texas gal

  • Newbie
  • Posts: 1
hello new to the board
« on: February 20, 2015, 11:19:25 am »
hello,  I am genotype 1A. diagnosed in 1996. Most likely have had it since early 80's.  In 2004-2005 Interferon and ribavirin treatment.  Cleared then immediately came back,  Treatment killed me.  Recently I starting feeling way worse with  new gastro issues along with the on going fatigue, bone joint paint (trigger fingers), shortness of breath and we can go on with a long list....  So, end of 2014  Endoscope found Grade 1 Varices and Moderate Portal Hypertensive Gastropathy.   After that my dr. met with me and we discussed Harvoni and started the process for a 24 week  treatment.  I am suppose to find out soon what insurance said.    We had to fight for the interferon/ribos.   
I have some questions.   I have a new work position so....

1.  How often do you have to see Dr. or go in for blood work while on Harvoni.
2. After treatment and you have cleared do most start feeling better ? 

thank you





Offline lporterrn

  • Member
  • Posts: 1,969
  • LucindaPorterRN
    • LucindaPorterRN
Re: hello new to the board
« Reply #1 on: February 20, 2015, 01:53:02 pm »
Welcome. I think you will notice a huge difference between treatments. Here are the lab recommendations: http://www.hcvguidelines.org/full-report/monitoring-patients-who-are-starting-hepatitis-c-treatment-are-treatment-or-have

I felt better quickly, but gradually. It took awhile for the brain fog to clear. Everyone is different.
Lucinda Porter, RN
1988 Contracted HCV
1997 Interferon nonresponder
2003 PEG + ribavirin responder-relapser
2013 Cured (Harvoni + ribavirin clinical trial)
https://www.hepmag.com/blogger/lucindakporter

 


© 2024 Smart + Strong. All Rights Reserved.   terms of use and your privacy
Smart + Strong® is a registered trademark of CDM Publishing, LLC.